ACE Report Cover
Arthroscopic acromioplasty may not be efficacious for shoulder impingement syndrome
Translate this  ACE Report Translate this  ACE Report Translate this  ACE Report
Lingua
Download Download Download
Scaricare
Cite this Report Cite this Report Cite this Report
Citare
Add to Favorites Add to Favorites Add to Favorites Remove from Favorites Remove from Favorites Remove from Favorites
+ Preferiti
Translate this  ACE Report Translate this  ACE Report Translate this  ACE Report
Lingua
Download Download Download
Scaricare
Cite this Report Cite this Report Cite this Report
Citare
Add to Favorites Add to Favorites Add to Favorites Remove from Favorites Remove from Favorites Remove from Favorites
+ Preferiti
SHOULDER & ELBOW
Arthroscopic acromioplasty may not be efficacious for shoulder impingement syndrome .
Verified
This report has been verified by one or more authors of the original publication.

OrthoEvidence Journal (OE Journal) - ACE Report

OE Journal. 2016;4(6):45 Acta Orthop. 2015 Dec;86(6):641-6
Autori che hanno contribuito

S Ketola J Lehtinen T Rousi M Nissinen H Huhtala I Arnala

140 patients with shoulder impingement syndrome were randomized to either a supervised exercise program alone or to arthroscopic acromioplasty followed with a similar exercise program. The purpose of this subgroup analysis study was to determine which patients (from either the arthroscopic acromioplasty and exercise therapy group, or the group treated solely with exercise therapy) are effectively treated for shoulder impingement syndrome when followed up at 2 and 5 years. Findings showed similar results between the patients who underwent operative treatment and the group that underwent conservative treatment. Furthermore, arthroscopic acromioplasty did not appear to improve results in patients who were originally allocated to exercise therapy alone and were unsatisfied with outcome following conservative management.


Dettagli sul finanziamento della pubblicazione +
Finanziamento:
Non-Industry funded
Sponsor:
Professor of medicine Y. T. Konttinen from Helsinki University Central Hospital
Conflicts:
None disclosed

Rischio di pregiudizio

4/10

Criteri di segnalazione

16/20

Indice di fragilità

N/A

Was the allocation sequence adequately generated?

Was allocation adequately concealed?

Blinding Treatment Providers: Was knowledge of the allocated interventions adequately prevented?

Blinding Outcome Assessors: Was knowledge of the allocated interventions adequately prevented?

Blinding Patients: Was knowledge of the allocated interventions adequately prevented?

Was loss to follow-up (missing outcome data) infrequent?

Are reports of the study free of suggestion of selective outcome reporting?

Were outcomes objective, patient-important and assessed in a manner to limit bias (ie. duplicate assessors, Independent assessors)?

Was the sample size sufficiently large to assure a balance of prognosis and sufficiently large number of outcome events?

Was investigator expertise/experience with both treatment and control techniques likely the same (ie.were criteria for surgeon participation/expertise provided)?

Sì = 1

Incerto = 0,5

Non rilevante = 0

No = 0

La valutazione dei criteri di segnalazione valuta la trasparenza con cui gli autori riportano le caratteristiche metodologiche e sperimentali dello studio all'interno della pubblicazione. La valutazione è suddivisa in cinque categorie che vengono presentate di seguito.

3/4

Randomization

1/4

Outcome Measurements

4/4

Inclusion / Exclusion

4/4

Therapy Description

4/4

Statistics

Detsky AS, Naylor CD, O'Rourke K, McGeer AJ, L'Abbé KA. J Clin Epidemiol. 1992;45:255-65

L'Indice di Fragilità è uno strumento che aiuta l'interpretazione dei risultati significativi, fornendo una misura della forza di un risultato. L'Indice di Fragilità rappresenta il numero di eventi consecutivi che devono essere aggiunti a un risultato dicotomico per rendere il risultato non più significativo. Un numero piccolo rappresenta un risultato più debole, mentre un numero grande rappresenta un risultato più forte.

Perché questo studio era necessario ora?

Shoulder impingement syndrome is a common source of shoulder pain and functional deficit. Both operative and non-operative methods have been used to treat shoulder impingement syndrome. Despite previous literature suggesting that arthroscopic acromioplasty may not offer any significant advantages over exercise therapy, the use of arthroscopic acromioplasty in the treatment of shoulder impingement has been increasing over the past years. . This subgroup analysis was conducted to identify the individuals within the sample population that would benefit from operative treatment.

Qual era la domanda di ricerca principale?

What differences, if any, exist between subgroups of patients treated with acromioplasty and exercise therapy versus exercise therapy alone in the management of shoulder impingement syndrome, as assessed over a 5-year follow-up period?

Caratteristiche dello studio +
Population:
140 patients (18-60 years of age) with shoulder impingement syndrome. To be eligible for inclusion, patients must have symptoms that were unresponsive to previous nonoperative treatments, as well as a lack of previous shoulder surgery. (n=140; Mean age: 47 years; 52M/88F)
Intervention:
Combined group: patients in this group underwent combined treatment of arthroscopic acromioplasty followed by a structured exercise program. An arthroscopic decompression was initially performed for these patients. All patients were under regional anesthesia, and the operation was performed using a burr drill. (n=70; Mean age: 46.4 [Range: 23.3 to 60]; 41F/29M; 57 completed follow-up)
Comparison:
Exercise therapy group: patients randomized to this group only took part in the supervised exercise program. (n=70; Mean age: 47.8 [Range: 26.8 to 59.2]; 47F/23M; 52 completed follow-up)
Outcomes:
The primary outcome of this study was self-reported pain measured by a visual analogue scale (VAS). The number of pain-free patients was also determined by the criteria of having a VAS score of 3 or less from a scale of 0 to 10. Secondary outcomes consisted of disability measurements, working ability, VAS pain at night, shoulder disability questionnaire (SDQ) score and a number of reported days with pain before follow-up.
Methods:
RCT; single-center
Time:
Follow up was conducted at 2 and 5 years after randomization.
Quali erano i risultati importanti?
  • Both the operative and non-operative groups reported significant improvements compared to baseline for self-reported pain, disability, working ability, pain at night, SDQ score and reported days with pain. Outcomes were similar between the groups.
  • Patients who were dissatisfied in the non-operative group and later received operative treatment reported worse values compared to patients in the other groups.
  • Overall in the entire cohort, 86 patients were pain-free and 48 patients reported pain (>3 on a visual analog scale) at 2-year follow-up. At 5 years, 82 patients were pain-free and 27 patients reported pain.
  • A number of factors were identified as having a statistically significant impact on pain. At 2-year follow-up factors included: living alone (Odds ratio 3.29 [95%CI 1.39-7.78]), lack of professional education (OR 3.67 [95%CI 1.20-11.2]), moderate load lifted per day (20-100kg) (OR 4.36 [95%CI 1.38-13.8]), and sick leave prior to randomization exceeding 2 weeks (OR 2.52 [95%CI 1.10-10.22]). At 5-year follow-up factors included: living alone (OR 2.77 [95%CI 1.02-7.55]), moderate-heavy load lifted per day (100-500kg) (OR 4.35 [95%CI 1.13-18.1]), and sick leave prior to randomized exceeding 2 weeks (OR 3.83 [95%CI 1.35-10.9]).
  • Overall satisfaction at work demonstrated a statistically significant effect on pain at 2-year follow-up (p=0.01), and requirement/challenges at work demonstrated a statistically significant effect on pain at 5 years (p=0.01).
Che cosa devo ricordare di più?

In the treatment of shoulder impingement syndrome, similar results for self-reported pain, disability, working ability, pain at night, SDQ score, and reported days with pain were demonstrated between arthroscopic acromioplasty with exercise therapy compared to exercise therapy alone. Patients initially in the exercise therapy group that later wanted arthroscopic acromioplasty did not show postoperative improvement.

Come influenzerà l'assistenza ai miei pazienti?

Based on the results of this analysis, arthroscopic acromioplasty may not offer any significant difference in clinical outcome when compared to supervised exercise therapy, or in cases of pursued surgery following supervised exercise therapy. The authors also reported that there does not appear to be a specific subgroup of patients to guide the decision between supervised exercise therapy and arthroscopic acromioplasty. Future research should consider possible patient subgroups as enrollment criteria in order to prospectively analyze outcomes between supervised exercise therapy and arthroscopic acromioplasty with a more narrow focus, as opposed to a secondary analysis with low sample sizes for multiple variables.

DISCLAIMER

Il contenuto di questa pagina è solo a scopo informativo e non intende sostituire la consulenza, la diagnosi o il trattamento medico professionale. Se ha bisogno di cure mediche, si rivolga sempre al suo medico o al pronto soccorso più vicino. Le opinioni, le convinzioni e i punti di vista espressi dalle persone sui contenuti presenti in questa pagina non riflettono le opinioni, le convinzioni e i punti di vista di OrthoEvidence.

0 di 4 articoli mensili GRATUITI sbloccati
Ha raggiunto il suo limite di 4 visualizzazioni di articoli gratuiti questo mese

Accesso a OrthoEvidence a soli 1,99 dollari a settimana.

Rimanga in contatto con le ultime prove. Può disdire in qualsiasi momento.
  • Valutazioni critiche dei più recenti studi randomizzati controllati ad alto impatto e delle revisioni sistematiche in ortopedia.
  • Accesso ai contenuti del podcast OrthoEvidence, tra cui collaborazioni con il Journal of Bone and Joint Surgery, interviste con chirurghi di fama internazionale e tavole rotonde su notizie e argomenti ortopedici.
  • Abbonamento a The Pulse, una newsletter bisettimanale basata sulle evidenze scientifiche, progettata per aiutarla a prendere decisioni cliniche migliori.
Upgrade
Bentornato!
Ha dimenticato la password?
Inizi la sua prova gratuita oggi stesso!

Il suo account sarà affiliato a
e includerà l'accesso gratuito a OrthoEvidence


O
Ha dimenticato la password?

O
Controlli la sua e-mail

Se esiste un account con l'indirizzo e-mail fornito, le verrà inviata un'e-mail di reimpostazione della password. Se non vede l'e-mail, controlli la cartella spam o posta indesiderata.

Per ulteriore assistenza, contatti il nostro team di supporto.

Effettui il login per abilitare questa funzione

Per accedere a questa funzione, deve essere collegato ad un account OrthoEvidence attivo. Effettui il login o crei un account di prova GRATUITO.

Tradurre il Rapporto ACE

OrthoEvidence utilizza un servizio di traduzione di terze parti per rendere i contenuti accessibili in più lingue. Si prega di notare che, sebbene venga fatto ogni sforzo per garantire l'accuratezza, le traduzioni potrebbero non essere sempre perfette.

Come citare questo documento ACE Report

OrthoEvidence. Arthroscopic acromioplasty may not be efficacious for shoulder impingement syndrome. OE Journal. 2016;4(6):45. Available from: https://myorthoevidence.com/AceReport/Show/arthroscopic-acromioplasty-may-not-be-efficacious-for-shoulder-impingement-syndrome

Copiare la citazione
Effettui il login per abilitare questa funzione

Per accedere a questa funzione, deve essere collegato ad un account OrthoEvidence attivo. Effettui il login o crei un account di prova GRATUITO.

Funzionalità per i membri Premium

Per accedere a questa funzione, deve essere collegato ad un account OrthoEvidence Premium.

Condividi questo articolo ACE Report